PIPages
Labs

Robert Carrillo

University of Chicago, IL·Neuroscience·Early-career

How does each neuron find the right partner, and what happens to the rest of a circuit when one connection fails? Neurons connect at synapses, the junctions where they pass signals to other cells.

Fields

Neuroscience

Genetics

Biology

Topics

Drosophila

fruit fly

neuromuscular junction

Grants
2 known grants, through May 2027

What they work on

  1. Test how combinations of Dpr and DIP cell surface proteins tell Drosophila motor neurons which muscles to connect to, using single-cell genetic changes in motor neurons that express six DIPs.
  2. Create Dpr-DIP binding variants with stronger or weaker attraction to test whether binding on the same cell and across cells together sharpens synaptic partner choice.
  3. Identify a signaling pathway between neighboring axon branches that controls the size of each nerve-muscle junction (NMJ), using functional and genetic approaches.
  4. Test whether disrupting one motor neuron causes compensating structural and functional changes in other neurons connected to the same muscle, using genetic manipulations, calcium imaging and electrophysiology.

More about the research

Both questions are studied in a simple system with precise, repeatable wiring: the nerve-muscle connections of the fruit fly Drosophila larva. Here each muscle receives only a few motor neurons, and every synapse can be seen and measured.

Why it matters

Flies have Dpr and DIP proteins, and humans have related proteins called IgLONs. IgLONs help build neural circuits and have been linked to autism, schizophrenia and dyslexia. Learning how these proteins direct precise wiring, and how circuits compensate when one input fails, could lay the groundwork for future clinical approaches to these disorders.

Known grants

From NIH and NSF research grants. Labs often have other funding we can't see.

IgSF protein interactions drive specificity in circuit wiring and synaptic elaboration

NIH · Jun 2021 – May 2027

CAREER: Structural and Functional Plasticity Induced By Loss of a Co-Innervating Neuron

NSF · Mar 2021 – Feb 2027

Closest labs

David L. Van Vactor

Harvard University, MA·Neuroscience

Test how miR-219, a conserved microRNA, controls dRalGPS levels at the fly neuromuscular junction, using site-directed mutagenesis of its binding site and tissue-specific analysis in muscle.

Richard Sando

Vanderbilt University, TN·Neuroscience·Early-career

Determine the biological functions and intracellular signaling mechanisms of adhesion G-protein-coupled receptors (aGPCRs), cell-surface proteins that both glue neurons together and trigger signaling, building on the lab's finding that Latrophilins set synaptic wiring specificity in hippocampal CA1.

Osvaldo Delbono

Wake Forest University, NC·Neuroscience

Define how brainstem A5 sympathetic neurons projecting to hindlimb muscles affect motor denervation, neuromuscular junction signaling and muscle mass and strength with aging, using optogenetics and retrograde labeling in living mice.

The school

University of Chicago: 39 labs on PI Pages, $681M a year on research, 457 research doctorates a year.

More about University of Chicago

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